The aims of the aorta-stent-Registry are: • participating hospitals (with audit) document all consecutive patients diagnosed with a disease of the distal thoracal aorta that receive one of the following therapies:
1. Endovascular Aorta-Stent-Graft 2. Surgical operation of the distal thoracal aorta * Documentation of the indications, the procedural results and the clinical short- and long-term results of the endovascular and chirurgical treatment in day to day hospital routine. * Documentation of the operational risk (Euroscore) * Documentation of the technical enforcement of the procedure as well as the result of the intervention * Documentation of the hospital lethality and the non-fatal serious complications (Spinal Cord Ischemia, SCI, Stroke, TIA, high blood loss etc.) * Documentation of medication at hospital discharge * Documentation of long-term lethality and non-fatal serious complications (SCI, Stroke, TIA, major bleeding etc.) as well as hospitalization, re-intervention rates and medicinal drug therapy after 30 days, 1, 3 \& 5 years.
Study Type
OBSERVATIONAL
Enrollment
199
Herz-Zentrum Bad Krozingen
Bad Krozingen, Germany
Kerckhoff-Klinik GmbH
Bad Nauheim, Germany
Segeberger Kliniken GmbH
Bad Segeberg, Germany
Westdeutsches Herzzentrum Essen, Uniklinikum
Essen, Germany
◦Documentation of the indications, the procedural results and the clinical short- and long-term results of the endovascular and chirurgical treatment in day to day hospital routine
Time frame: Hospital-stay
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Klinikum Ludwigshafen
Ludwigshafen, Germany
Universitätsklinikum Magdeburg
Magdeburg, Germany
Städt. Klinikum München GmbH
München, Germany
Universitätsklinikum Rostock
Rostock, Germany